Evidence map›Paper›PMID 31782728›Full record

ArticleeLife2019

Endothelial EphB4 maintains vascular integrity and transport function in adult heart.

Guillermo Luxán, Jonas Stewen, Noelia Díaz, Katsuhiro Kato, Sathish K Maney, Anusha Aravamudhan, Frank Berkenfeld, Nina Nagelmann, Hannes Ca Drexler, Dagmar Zeuschner and 7 more

Abstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed.

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  20. Endothelial cell dysfunction in cardiac disease: driver or consequence?Frontiers in cell and developmental biology · 2023
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Guillermo Luxán *Department of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, Münster, Germany.ORCID 0000-0001-8350-8659
Jonas Stewen *Department of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Noelia DíazRegulatory Genomics Laboratory, Max Planck Institute for Molecular Biomedicine, Münster, Germany.ORCID 0000-0002-0319-3448
Katsuhiro KatoDepartment of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Sathish K ManeyDepartment of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Anusha AravamudhanDepartment of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Frank BerkenfeldDepartment of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Nina NagelmannDepartment of Clinical Radiology, University Hospital Münster, Münster, Germany.
Hannes Ca DrexlerBioanalytical Mass Spectrometry Unit, Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Dagmar ZeuschnerElectron Microscopy Unit, Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Cornelius FaberDepartment of Clinical Radiology, University Hospital Münster, Münster, Germany.ORCID 0000-0001-7683-7710
Hermann SchillersInstitute for Physiology II, University of Münster, Münster, Germany.
Sven HermannEuropean Institute for Molecular Imaging, University of Münster, Münster, Germany.
John WisemanDiscovery Biology, Discovery Sciences, IMED Biotech Unit, AstraZeneca, Gothenburg, Sweden.
Juan M VaquerizasRegulatory Genomics Laboratory, Max Planck Institute for Molecular Biomedicine, Münster, Germany.ORCID 0000-0002-6583-6541
Mara E Pitulescu *Department of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Ralf H Adams *Department of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, Münster, Germany.ORCID 0000-0003-3031-7677

Funding

Deutsche Forschungsgemeinschaft Cells-in-Motion Cluster of Excellence (EXC 1003-CiM) - Pilot Project PP-2015-12Deutsche Forschungsgemeinschaft SFB 1348 and Cells-in-Motion Cluster of Excellence (EXC 1003-CiM)EMBO Postdoctoral fellowship - ALTF 421-2014Max-Planck-Gesellschaft Open-access funding (CRC 1348)
6 · The paper itself

Abstract

The homeostasis of heart and other organs relies on the appropriate provision of nutrients and functional specialization of the local vasculature. Here, we have used mouse genetics, imaging and cell biology approaches to investigate how homeostasis in the adult heart is controlled by endothelial EphB4 and its ligand ephrin-B2, which are known regulators of vascular morphogenesis and arteriovenous differentiation during development. We show that inducible and endothelial cell-specific inactivation of

Indexed as

AdultAnimalsCell AdhesionCell DifferentiationEmbryonic DevelopmentEndothelial CellsEndothelium, VascularEphrin-B2HeartHomeostasisHumansLigandsMiceMorphogenesisMuscle, SkeletalNeovascularization, PhysiologicEFNB2 protein, mouseEphb4 protein, mouseEphrin-B2LigandsReceptor, EphB4blood vesselcardiomyocytedevelopmental biologyendothelial cellhearthomeostasismouse

Identifiers

PMID31782728
PMCPMC6884395

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.